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Completed Phase 1 Interventional

An Open-Label Study of Aripiprazole Lauroxil in Subjects With Stable Schizophrenia

ClinicalTrials.gov ID: NCT02320032

Public ClinicalTrials.gov record NCT02320032. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 3:17 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1, Randomized, Open-Label Study Evaluating the Pharmacokinetics of Various Dosing Regimens of Aripiprazole Lauroxil in Subjects With Stable Schizophrenia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will evaluate the safety, tolerability, and pharmacokinetics (PK) of various doses and dosing intervals of aripiprazole lauroxil.

Study identification

NCT ID
NCT02320032
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Alkermes, Inc.
Industry
Enrollment
140 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2014
Primary completion
Mar 31, 2016
Completion
Mar 31, 2016
Last update posted
Aug 28, 2018

2014 – 2016

United States locations

U.S. sites
16
U.S. states
9
U.S. cities
16
Facility City State ZIP Site status
Alkermes Investigational Site Little Rock Arkansas 72211
Alkermes Investigational Site Cerritos California 90703
Alkermes Investigational Site Garden Grove California 92845
Alkermes Investigational Site Washington D.C. District of Columbia 20016
Alkermes Investigational Site Lauderhill Florida 33161
Alkermes Investigational Site Leesburg Florida 34748
Alkermes Investigational Site Maitland Florida 32751
Alkermes Investigational Site Oakland Park Florida 33334
Alkermes Investigational Site Tampa Florida 33613
Alkermes Investigational Site Atlanta Georgia 30308
Alkermes Investigational Site Chicago Illinois 60640
Alkermes Investigational Site Hoffman Estates Illinois 60169
Alkermes Investigational Site St Louis Missouri 63118
Alkermes Investigational Site Marlton New Jersey 8053
Alkermes Investigational Site Austin Texas 78754
Alkermes Investigational Site Dallas Texas 75243

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02320032, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 28, 2018 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02320032 live on ClinicalTrials.gov.

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